Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Mitchell E. Taub"'
Autor:
Jonathan A. Phillips, Mitchell E. Taub, Matthew S. Bogdanffy, Jing Yuan, Brian Knight, James D. Smith, Warren W. Ku
Publikováno v:
Journal of Applied Toxicology. 42
Autor:
Jonathan A. Phillips, Mitchell E. Taub, Matthew S. Bogdanffy, Jing Yuan, Brian Knight, James D. Smith, Warren W. Ku
Publikováno v:
Journal of applied toxicology : JATREFERENCES. 42(10)
Inhibition of sodium-glucose cotransporter-2 (SGLT2) has been shown to be a safe and efficacious approach to support managing Type 2 diabetes. In the 2-year carcinogenicity study with the SGLT2 inhibitor empagliflozin in CD-1 mice, an increased incid
Autor:
Sabrina Wiebe, Ashish Sharma, Martin F. Fromm, Alen Jambrecina, Peter Stopfer, Fabian Müller, Edith Hauel, Kerstin Bader, Mitchell E. Taub, Gerd Mikus, Kathrin Hohl, Sven Schmidt-Gerets, Thomas Giessmann, Thomas Ebner, Naoki Ishiguro
Publikováno v:
Clinical Pharmacokinetics
Background and Objective A novel cocktail containing four substrates of key drug transporters was previously optimized to eliminate mutual drug–drug interactions between the probes digoxin (P-glycoprotein substrate), furosemide (organic anion trans
Publikováno v:
Drug Metabolism and Disposition. 48:690-697
Long-term hepatocyte culture systems such as HepatoPac are well suited to evaluate the metabolic turnover of low clearance (CL) drugs because of their sustained metabolic capacity and longer-term viability. Erythromycin (ERY), a moderate, mechanism-b
Autor:
Chukwunonso K Nwabufo, Iain Martin, Matthew Segall, Fabio Broccatelli, Emily E. Scott, Eric Gonzalez, Jasleen K. Sodhi, Laura E Russell, Aaron G. Bart, Mary A. Schleiff, W. Griffith Humphreys, Ryan H. Takahashi, Mitchell E. Taub, Volker M. Lauschke, Bhagwat Prasad, Jessica H. Hartman
Publikováno v:
Drug Metab Rev
The 12(th) International Society for the Study of Xenobiotics (ISSX) meeting, held in Portland, OR, USA from July 28–31, 2019, was attended by diverse members of the pharmaceutical sciences community. The ISSX New Investigators Group provides learn
Autor:
Bhagwat Prasad, Peter Stopfer, Valerie Nock, Hannah Britz, Thorsten Lehr, Mitchell E. Taub, Éric Fernandez, Ting Wang, Nina Hanke
Publikováno v:
Pharmaceutical Research
PurposeTo provide whole-body physiologically based pharmacokinetic (PBPK) models of the potent clinical organic anion transporter (OAT) inhibitor probenecid and the clinical OAT victim drug furosemide for their application in transporter-based drug-d
Publikováno v:
Drug Metabolism and Disposition. 46:770-778
BI 187004, an 11β-hydroxysteroid dehydrogenase 1 inhibitor, was administered once daily for 14 days to eight patients with type 2 diabetes mellitus. N-methylation was identified as a major biotransformation pathway. In four patients treated with BI
Autor:
Jonathan A. Phillips, Hlaing Hlaing Maw, Warren W. Ku, Hongbin Yu, Patricia A. Escobar, William T. Loging, Mitchell E. Taub, Zimei Huang, Pamela Foppiano, James D. Smith
Publikováno v:
International Journal of Toxicology. 36:440-448
In a previously reported CD-1 mouse 2-year carcinogenicity study with the sodium glucose cotransporter-2 inhibitor empagliflozin, an increased incidence of renal tubular adenomas and carcinomas was identified only in the male high-dose group. Follow-
Autor:
Kathrin Hohl, Naoki Ishiguro, Thomas Giessmann, Ashish Sharma, Arvid Jungnik, Mitchell E. Taub, Dietmar Gansser, Thomas Ebner, Peter Stopfer, Fabian Müller
Publikováno v:
European Journal of Drug Metabolism and Pharmacokinetics
In a recently described probe drug cocktail for clinically relevant drug transporters containing digoxin, furosemide, metformin and rosuvastatin, mutual interactions were essentially absent except for increases in the systemic exposure of rosuvastati
Autor:
Naoki Ishiguro, Mitchell E. Taub, H Zimdahl-Gelling, Dietmar Gansser, Kathrin Hohl, Thomas Giessmann, Thomas Ebner, Ashish Sharma, M Wein, Peter Stopfer, Fabian Müller
Publikováno v:
Clinical Pharmacology and Therapeutics
This article reports the clinical investigation of a probe drug cocktail containing substrates of key drug transporters. Single oral doses of 0.25 mg digoxin (P-gp), 5 mg furosemide (OAT1 and OAT3), 500 mg metformin (OCT2, MATE1, and MATE2-K), and 10